Phenylephrine resinate particles having good auc

ABSTRACT

Phenylephrine particles suitable for solid, semi solid or liquid dosage forms are disclosed.

FIELD OF THE INVENTION

The present invention relates to phenylephrine particles suitable forsolid, semi solid or liquid dosage forms. The phenylephrine particles,which may be coated, release phenylephrine at rates that providepharmaceutically suitable plasma concentrations for an extended periodof time. The present invention also relates to a process formanufacturing dosage forms containing the phenylephrine particles and tomethods for alleviating nasal and respiratory congestion in humansubjects with the oral administration of the dosage forms. The dosageforms can further comprise one or more additional therapeutically activeagents selected from one or more of the group consisting ofantihistamines, decongestants, analgesics, anti-inflammatories,anti-pyretics, cough suppressants and expectorants.

BACKGROUND OF THE INVENTION

Phenylephrine is a potent vasoconstrictor, possessing both direct andindirect sympathomimetic effects [Hoffman 2001]. The dominant and directeffect is agonism at al-adrenergic receptors. Stimulation ofal-adrenergic receptors located on capacitance blood vessels of thenasal mucosa (postcapillary venules) results in vasoconstriction,decreased blood volume, and a decrease in the volume of the nasal mucosa(nasal decongestion) [Johnson 1993]. Constricted blood vessels allowless fluid to enter the nose, throat, and sinus linings, which resultsin decreased inflammation of nasal membranes as well as decreased mucousproduction [Johnson 1993]. Thus, by constriction of blood vessels,mainly those located in the nasal passages, phenylephrine causes adecrease in nasal congestion [Hoffman 2001, Empey 1981].

Phenylephrine is a Category I (Generally Regarded as Safe and Effective(GRASE)) over-the-counter (OTC) oral nasal decongestant. Globally,phenylephrine has been available since the 1960's, and since 1996,phenylephrine has been widely used in the United States. Phenylephrinehydrochloride, which is widely used in OTC adult and pediatric cough andcold medicines, is indicated for use by adults and children for thetemporary relief of nasal congestion due to the common cold, hay fever,or other upper respiratory allergies (allergic rhinitis). It iscommercially available in 10 mg tablets for oral administration inadults. The dosing regimen is one 10 mg dose of phenylephrine every fourhours, not to exceed 60 mg (six doses) in 24 hours. Complete informationis available in the OTC monograph labeling for approved drugs.

Phenylephrine, chemical name(R)-1-(3-hydroxyphenyl)-2-methylaminoethanol, is commercially availableas a hydrochloride salt. The empirical formula is C9H13NO2.HCl and themolecular weight is 203.67. The compound, which is a white to off-whitecrystalline powder, has the following chemical structure:

The principal routes of phenylephrine metabolism are sulfate conjugation(mainly in the intestinal wall) and oxidative deamination by both the Aand B forms of monoamine oxidase [Suzuki 1979]. Glucuronidation alsooccurs, but to a lesser extent. In one study, following a 30 mg doseadministered orally over eight hours [Ibrahim 1983], phenylephrine wasmetabolized to phenylephrine-sulfate, m-hydroxymandelic acid,phenylephrine-glucuronide and m-hydroxy-phenylglycol-sulfate at 47%,30%, 12%, and 6% of the dose, respectively. Deamination is thepredominant metabolic pathway after intravenous injection ofphenylephrine [Hengstmann 1982], whereas sulfate conjugation is thepredominant pathway after oral administration. Phase I and Phase IImetabolites of phenylephrine in humans are shown below. The percentagevalues in the schematic refer to the percent of an oral dose as reportedby Ibrahim.

Efficacy data from clinical trials of immediate-release phenylephrineuse in adults indicate that phenylephrine is an effective nasaldecongestant.

Acetaminophen is a para-aminophenol derivative with analgesic andantipyretic activity. It is used for the temporary relief of minor achesand pains associated with the common cold, backache, headache,toothache, menstrual cramps, and muscular aches; and for the temporaryrelief of the minor pain of arthritis and for the reduction of fever.The adult dose of acetaminophen in the United States is 1000 mg everyfour to six hours with a maximum of 4000 mg in 24 hours. The adult doseof extended release acetaminophen is 1300 mg every eight hours with amaximum of 3900 mg in 24 hours.

Acetaminophen is primarily metabolized by the liver via three majorparallel pathways: glucuronidation, sulfation, and oxidation [Miners1983; Slattery 1989; Lee 1992; Miners 1992]. Both the glucuronic andoxidative pathways adhere to a first-order rate process, which means theconcentration of acetaminophen metabolized increases as theconcentration in the liver increases.

The sulfate pathway adheres to Michaelis-Menten kinetics, which meansthe concentration of acetaminophen metabolized remains constant once theconcentration in the liver increases above a saturation level.

A schematic of acetaminophen metabolism is shown below. Less than 9% ofa therapeutic dose is excreted unchanged in the urine [Miners 1992]. Themajor metabolic pathway is glucuronidation, where 47% to 62% of theacetaminophen dose conjugates with glucuronide. These glucuronideconjugates are inactive and nontoxic [Koch-Weser 1976], and are secretedin bile and eliminated in the urine. Glucuronide conjugation iscatalyzed primarily by one isoform of glucuronyltransferase (UGT1A6)[Court 2001] with uridine 5′-diphosphoglucuronic acid as an essentialcofactor.

The second major pathway of acetaminophen metabolism is sulfation, where25% to 36% of the dose conjugates with sulfate. These sulfate esterconjugates are also inactive and nontoxic [Koch-Weser 1976], and arereadily excreted in the urine. Sulfation is mediated bysulfotransferases, which are heterogeneous cytosolic enzymes, and3′-phosphoadenosine 5′-phosphate is a cofactor. Sulfotransferaseactivity rather than sulfate depletion is the rate-controlling factor ofacetaminophen sulfation [Blackledge 1991].

The third pathway is oxidation, where 5% to 8% of the acetaminophen doseis metabolized via the cytochrome P-450 enzyme system. The cytochromeP-450 isoenzyme that is primarily responsible for acetaminophenmetabolism is CYP2E1 [Manyike 2000]. When acetaminophen is metabolizedby CYP2E1, it forms a highly reactive intermediate,N-acetyl-p-benzoquinoneimine (NAPQI). Because NAPQI is highly reactive,it cannot be measured outside the liver nor can it accumulate. Thisintermediate is rapidly inactivated by hepatocellular stores ofglutathione to form cysteine and mercapturate conjugates, which are bothinactive and nontoxic [Koch-Weser 1976]. These conjugates are excretedin the urine [Mitchell 1974].

There is a need for less frequent delivery of phenylephrine. Lessfrequent administration results in improved patient compliance. Inaddition, constant therapeutic plasma levels of active components can bemore effective and even efficacious compared to the fluctuations seenwhen multiple doses of a conventional immediate release formulation aregiven. Sustained effective levels could decrease the severity andfrequency of side effects seen with high peak plasma levels. Thus,formulations of phenylephrine that can be administered less frequently,for example, once every 6, 8, 12, 16, 20, or 24 hours, are needed.

There is also a need to match the duration of phenylephrine with activesthat provide a longer duration than immediate release phenylephrine.

U.S. Published Application No. 20070281020 to Schering-PloughCorporation discloses the administration of a sustained release tabletcomprising 30 mg phenylephrine, hydroxypropyl methylcellulose,carboxymethyl cellulose sodium, Kollidon CL-M, colloidal silicon dioxideand magnesium stearate to a human subject and the comparison of thesustained release tablet to three doses of 10 mg immediate releasephenylephrine.

U.S. Pat. No. 8,282,957 to McNeil-PPC, Inc. discloses coatedphenylephrine particles containing phenylephrine HCl, modified starchand Eudragit NE30D™ coated with a first coating layer comprisingEudragit RS PO, acetyltributylcitrate and magnesium stearate and asecond coating layer comprising Eudragit NE30D™, Eudragit FS30D™,magnesium stearate, sodium lauryl sulfate and simethicone, and usethereof in pharmaceutical dosage forms, including dosage formscontaining acetaminophen.

U.S. Pat. No. 6,001,392 to Warner Lambert Company discloses a drug/resincomplex that contains a mixture of coated and uncoated Amberlite™ IR69cross-linked with divinylbenzene.

U.S. Published Application No. 20100068280 to Schering-PloughCorporation discloses pharmaceutical dosage forms comprisingphenylephrine in sustained release form. According to an embodiment, asingle dose of phenylephrine in a tablet containing 30 mg phenylephrine,lactose monohydrate, Methocel K100M CR, Klucel EXF and magnesiumstearate was compared to two 10 mg phenylephrine immediate releasetablets dosed 4 hours apart in a bioequivalence study.

U.S. Published Applications Nos. 20050266032 and 20060057205 toSovereign Pharmaceuticals disclose pharmaceutical dosage formscontaining phenylephrine. According to an embodiment, the phenylephrineis incorporated into an ion-exchange resin complex using, e.g., sodiumpolystyrene sulfonate, and coated with delayed release polymer, e.g.,Eudragit® L 100, Kollidon® MAE and Aquacoat® cPD. The formula in thisembodiment contains 45 mg sustained release phenylephrine and 15 mgimmediate release phenylephrine.

U.S. Pat. No. 8,062,667 to Tris Pharma, Inc. discloses coated drug-ionexchange resin complexes. According to an embodiment, phenylephrine isincorporated into an ion-exchange resin complex using, sodiumpolystyrene sulfonate, and coated with KOLLICOAT™ SR-30D, triacetin andwater.

U.S. Pat. No. 8,394,415 to McNeil-PPC, Inc. discloses a liquidformulation comprising immediate release ibuprofen and an extendedrelease phenylephrine-specified ion exchange resin complex coated withfirst and second coating layers comprising specified ingredients.

U.S. application Ser. No. 11/761,698 to McNeil-PPC, Inc. discloses asolid composition comprising ibuprofen (IR) and phenylephrine coatedwith first coating layer comprising ethylcellulose and second coatinglayer comprising protective coating.

U.S. Application No. 20100068280 to Schering-Plough Healthcare Products,Inc. discloses a bioavailability study that compared 10 mg phenylephrineHCl delivered via Enterion™ capsules, 10 mg Sudafed PE™ and 30 mgphenylephrine HCl delivered via Enterion™ capsules.

U.S. Patent Application No. 2007014239 to Coating Place, Inc. disclosesa method and composition for loading one or more drugs onto one or moreion exchange resin particles to form a drug loaded resin particle.

There continues to be a need for phenylephrine products having theattributes discussed above.

SUMMARY OF THE INVENTION

The present invention is directed to phenylephrine particles thatdeliver phenylephrine or a pharmaceutically acceptable salt thereof to asubject in need thereof so as to provide a peak plasma concentration ofphenylephrine at about 0.1 to about 16 hours, preferably about 0.5 toabout 5 hours, more preferably about 1 to about 4.5 hours, afteringestion and wherein the phenylephrine is maintained at a level greaterthan about 20, about 40, about 60, about 80, about 100, about 120, about140, about 160, about 180, or about 200, pg/mL for at least about 6,about 8, about 12, about 16, about 20 and/or about 24 hours afteringestion.

In accordance with a preferred embodiment, the invention is directed tocoated phenylephrine resinate particles that deliver phenylephrine or apharmaceutically acceptable salt thereof to a subject in need thereof soas to provide a peak plasma concentration of phenylephrine at about 0.1to about 16 hours, preferably about 0.5 to about 5 hours, morepreferably about 1 to about 4.5 hours, after ingestion and wherein thephenylephrine is maintained at a level greater than about 20, about 40,about 60, about 80, about 100, about 120, about 140, about 160, about180, or about 200, pg/mL for at least about 6, about 8, about 12, about16, about 20 and/or about 24 hours after ingestion.

The present invention is also directed to pharmaceutical dosage formscomprising phenylephrine particles that deliver phenylephrine or apharmaceutically acceptable salt thereof to a subject in need thereof soas to provide a peak plasma concentration of phenylephrine at about 0.1to about 16 hours, preferably about 0.5 to about 5 hours, morepreferably about 1 to about 4.5 hours, after ingestion and wherein thephenylephrine is maintained at a level greater than about 20, about 40,about 60, about 80, about 100, about 120, about 140, about 160, about180 or about 200, pg/mL for at least about 6, about 8, about 12, about16, about 20 and/or about 24 hours after ingestion.

In another embodiment, the phenylephrine particles, which provideextended release of phenylephrine, are combined with phenylephrine inimmediate release form.

In another embodiment, the phenylephrine particles are combined with oneor more additional therapeutic agent(s) for immediate or sustainedrelease. Such agent or agents may be formulated for immediate releaseupon ingestion, for sustained release, for release in the colonconcomitantly with at least some of the phenylephrine, or anycombination thereof. In one embodiment, the additional therapeutic agentis uncoated. In another embodiment, the additional therapeutic agent iscoated.

The additional therapeutic agent may be an antihistamine, adecongestant, an analgesic, an anti-inflammatory, an anti-pyretic, acough suppressant, an expectorant, or any other therapeutic agent orcombinations of such agents useful to alleviate the symptoms of a cold,seasonal and other allergies, hay fever, or sinus problems, any of whichmay cause an increase in nasal discharge. Preferably, the one or moreadditional therapeutic agents are acetaminophen.

Examples of antihistamines and decongestants, include, but are notlimited to, bromopheniramine, chlorcyclizine, dexbrompheniramine,bromhexane, phenindamine, pheniramine, pyrilamine, thonzylamine,pripolidine, ephedrine, pseudoephedrine, phenylpropanolamine,chlorpheniramine, dextromethorphan, diphenhydramine, doxylamine,astemizole, terfenadine, fexofenadine, naphazoline, oxymetazoline,montelukast, propylhexadrine, triprolidine, clemastine, acrivastine,promethazine, oxomemazine, mequitazine, buclizine, bromhexine,ketotifen, terfenadine, ebastine, oxatamide, xylomeazoline, loratadine,desloratadine, and cetirizine; isomers thereof, and pharmaceuticallyacceptable salts and esters thereof.

Examples of suitable analgesics, anti-inflammatories, and antipyreticsinclude, but are not limited to, non-steroidal anti-inflammatory drugs(NSAIDs) such as propionic acid derivatives (e.g., ibuprofen, naproxen,ketoprofen, flurbiprofen, fenbufen, fenoprofen, indoprofen, ketoprofen,fluprofen, pirprofen, carprofen, oxaprozin, pranoprofen, and suprofen)and COX inhibitors such as celecoxib; acetaminophen; acetyl salicylicacid; acetic acid derivatives such as indomethacin, diclofenac,sulindac, and tolmetin; fenamic acid derivatives such as mefanamic acid,meclofenamic acid, and flufenamic acid; biphenylcarbodylic acidderivatives such as diflunisal and flufenisal; and oxicams such aspiroxicam, sudoxicam, isoxicam, and meloxicam; isomers thereof, andpharmaceutically acceptable salts and prodrugs thereof.

Examples of cough suppressants and expectorants include, but are notlimited to, diphenhydramine, dextromethorphan, noscapine, clophedianol,menthol, benzonatate, ethylmorphone, codeine, acetylcysteine,carbocisteine, ambroxol, belladona alkaloids, sobrenol, guaiacol, andguaifenesin; isomers thereof, and pharmaceutically acceptable salts andprodrugs thereof.

Another aspect of the invention is a method of treating the symptoms ofcold, influenza, allergies, or non-allergic rhinitis in a subject inneed thereof comprising administering the phenylephrine particles of theinvention. In certain embodiments, the phenylephrine particles areadministered about every 6, 8, 12, 16, 20, or 24 hours. In one preferredembodiment, the phenylephrine particles are administered about every 12hours. In another preferred embodiment, the phenylephrine resinateparticles are administered about every 8 hours.

Certain embodiments of the invention are methods of maintainingsustained bioavailability of phenylephrine in a subject, comprisingorally administering to the subject phenylephrine particles, wherein atleast a portion of phenylephrine is absorbed from the colon, and whereinthe concentration of phenylephrine in the plasma of the subject is atleast about 20, about 40, about 60, about 80, about 100, about 120,about 140, about 160, about 180, or about 200, pg/mL at about 6 hoursafter administration of the composition. In particular embodiments, theconcentration of phenylephrine in the plasma of the subject is at leastabout 20, about 40, about 60, about 80, about 100, about 120, about 140,about 160, about 180, or about 200, pg/mL at about 8 hours afteradministration of the composition. In particular embodiments, theconcentration of phenylephrine in the plasma of the subject is at leastabout 20, about 40, about 60, about 80, about 100, about 120, about 140,about 160, about 180, or about 200, pg/mL at about 12 hours afteradministration of the composition. In particular embodiments, theconcentration of phenylephrine in the plasma of the subject is at leastabout 20, about 40, about 60, about 80, about 100, about 120, about 140,about 160, about 180, or about 200, pg/mL at about 20 hours afteradministration of the composition. In particular embodiments, theconcentration of phenylephrine in the plasma of the subject is at leastabout 20, about 40, about 60, about 80, about 100, about 120, about 140,about 160, about 180, or about 200, pg/mL at about 24 hours afteradministration of the composition. Certain other embodiments of theinvention are methods of administering phenylephrine to a subject,comprising orally administering phenylephrine particles, saidcomposition delivering at least some of the phenylephrine to the colonwhere phenylephrine is released in the colon and absorbed from thecolon.

The present invention may be more fully understood by reference to theFigures, Detailed Description and Examples which follow.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the mean plasma concentration profile of phenylephrine uponadministration of coated extended release (ER) phenylephrine resinateparticles containing 20 mg phenylephrine. Referring to FIG. 1, the yaxis represents the concentration of free phenylephrine in plasma inpicograms (pg) per milliliter (mL). The x axis represents time in hours.FIG. 1 shows that the average concentration of phenylephrine reached apeak (Cmax) at about 2 hours. FIG. 1 also shows a secondary peak atabout 12 hours.

FIG. 2 shows the individual plasma concentration profiles ofphenylephrine upon administration of coated ER phenylephrine resinateparticles containing 20 mg phenylephrine. Referring to FIG. 2, theintersubject variability is good for modified release phenylephrine. Therange of Cmax occurred from about 1 hour to about 4.5 hours. Thesecondary peak at about 12 hours was observed for all subjects.

FIG. 3 shows the mean plasma concentration profile of phenylephrine uponadministration of coated ER phenylephrine HCl particles containing 20 mgphenylephrine. Referring to FIG. 3, the dashed line is the profile fromFIG. 1 for comparison purposes. A slightly higher Cmax with thephenylephrine resinate particles was observed. A secondary peak at about12 hours is observed in both profiles. This may be the result of lessphenylephrine being metabolized presystemically by the gut wall as aresult of the particles quick movement down the GI tract. Release ofphenylephrine in the colon would result in higher absorption at a latertime.

FIG. 4 shows the individual plasma concentration profiles ofphenylephrine upon administration of coated ER phenylephrine HClparticles containing 20 mg phenylephrine.

FIG. 5 shows the mean plasma concentration profile of phenylephrine uponadministration of coated ER phenylephrine resinate particles containing15 mg phenylephrine and liquid IR phenylephrine HCl containing 5 mgphenylephrine (the “ER-IR blend”). Referring to FIG. 5, the unbrokenline represents the ER-IR blend. Again, the curve for this treatment isconsistent with what was seen with the resinate and the HClformulations. For the ER-IR blend, there are two peaks within the first2 hours; one mainly from the IR dose and the other from the accumulationof the IR and ER doses. The Cmax was reached faster and maintained for alonger period of time. An ER-IR blend thus appears beneficial in termsof onset of efficacy.

FIG. 6 shows the individual plasma concentration profiles ofphenylephrine upon administration of coated ER phenylephrine resinateparticles containing 15 mg phenylephrine and liquid IR phenylephrine HClcontaining 5 mg phenylephrine.

FIG. 7 shows the mean plasma concentration profile of phenylephrine uponadministration of liquid IR phenylephrine HCl containing 20 mgphenylephrine. Referring to FIG. 7, the unbroken line represents theprofile for the currently marketed IR liquid product and the dashed lineis the profile from FIG. 5 for comparison. The Cmax of the ER-IR blendis lower than the Cmax of the IR form.

FIG. 8 shows the individual plasma concentration profiles ofphenylephrine upon administration of liquid IR phenylephrine HClcontaining 20 mg phenylephrine.

FIG. 9 shows the mean plasma concentration profile of phenylephrine uponadministration of coated ER phenylephrine resinate particles containing22.5 mg phenylephrine and liquid IR phenylephrine HCl containing 7.5 mgphenylephrine (the “ER-IR blend”) and compares to liquid IRphenylephrine HCl containing 20 mg phenylephrine.

FIGS. 10A and 10B compare the mean plasma concentration profile ofphenylephrine (1) upon administration of coated ER phenylephrineresinate particles containing 15 mg phenylephrine and liquid IRphenylephrine HCl containing 5 mg phenylephrine (FIG. 10A) and (2) uponadministration of coated ER phenylephrine resinate particles containing22.5 mg phenylephrine and liquid IR phenylephrine HCl containing 7.5 mgphenylephrine (FIG. 10B) with (3) liquid IR phenylephrine HCl containing20 mg phenylephrine.

FIG. 11 compares the mean plasma concentration profiles of phenylephrineupon administration of (1) coated ER phenylephrine resinate particlescontaining 15 mg phenylephrine and liquid IR phenylephrine HClcontaining 5 mg phenylephrine with a (2) combination of (a) coated ERphenylephrine resinate particles containing 15 mg phenylephrine, (b)liquid IR phenylephrine HCl containing 5 mg phenylephrine and (c) 1300mg ER acetaminophen.

DETAILED DESCRIPTION OF THE INVENTION

It is believed that one skilled in the art can, based upon thedescription herein, utilize the present invention to its fullest extent.The following specific embodiments are to be construed as merelyillustrative, and not as limiting the remainder of the disclosure in anyway whatsoever.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which the invention belongs. Also, all publications, patentapplications, patents, and other references mentioned herein areincorporated by reference. As used herein, all percentages are by weightunless otherwise specified. In addition, all ranges set forth herein aremeant to include any combinations of values between the two endpoints,inclusively.

DEFINITIONS

As used herein a pharmaceutically acceptable salt of phenylephrineincludes, but is not limited to, phenylephrine hydrochloride,phenylephrine bitartrate, phenylephrine tannate, etc. In one preferredembodiment, the pharmaceutically acceptable salt of phenylephrine isphenylephrine hydrochloride.

“AUC” as used herein means, for any given drug, the “area under theconcentration-time curve” from dosing or activation of the drug to atime point, calculated by the trapezoidal rule. AUC is a parametershowing the cumulative plasma concentration of a drug over time, and isan indicator of the total amount and availability of a drug in theplasma.

“Cmax” as used herein means the maximum (or peak) concentration that adrug achieves in tested area after the drug has been administrated andprior to the administration of a second dose.

As used herein, “crystalline form” shall mean the non-amorphous form ofthe active ingredient such that it displays crystal like propertiesincluding, but not limited to, the ability to diffract visible light.Crystalline may also be used to describe an active ingredient in itspure form, i.e., e.g., without the addition of other excipients thereto.

By “delayed release,” it is meant that, after administration, there isat least one period of time when an active ingredient is not beingreleased from the dosage form, i.e., the release of the activeingredient(s) occurs at a time other than immediately following oraladministration.

As used herein, “dissolution medium” shall mean any suitable liquidenvironment in which the suspension dosage form of the present inventioncan be dissolved, such as, for example, the in vitro dissolution mediaused for testing of the product, or gastro-intestinal fluids. Suitablein vitro dissolution media used for testing the dissolution of theactive ingredient or ingredients from the suspension dosage form of thepresent invention include those described in the United StatesPharmacopeia.

A “dosage”, “dosage form” or “dose” as used herein means the amount of apharmaceutical composition comprising therapeutically active agent(s)administered at a time. “Dosage”, “dosage form” or “dose” includesadministration of one or more units of pharmaceutical compositionadministered at the same time. In one embodiment, the dosage form is atablet. In one embodiment the dosage form is a multilayer tablet. In theembodiment comprising a multilayer tablet, one layer may comprise animmediate release portion and another layer may comprise an extendedrelease portion. In the embodiment comprising a multilayer tablet, onelayer may comprise the phenylephrine resinate particles, and anotherlayer may comprise an immediate release form of phenylephrine and/or asecond active ingredient. In one embodiment the dosage form comprisingphenylephrine resinate particles is a liquid filled soft-gel.

As used herein “drug-resin complex” shall mean the bound form of anactive ingredient, including but not limited to the pharmaceuticalactive ingredients, and an ion exchange resin. The drug-resin complex isalso referred to in the art as a “resinate.” An ion exchange resin thatmay be used in accordance with the invention is Amberlite™ IRP 69, TheDow Chemical Company, an insoluble, strongly acidic, sodium formcationic exchange resin derived from sulfonated copolymer of styrene anddivinylbenzene. The mobile, or exchangeable cation is sodium, which canbe exchanged for, or replaced by, many cationic (basic) species,including, e.g., copper, zinc, iron, calcium, strontium, magnesium andlithium. Adsorption of drug onto ion exchange resin particles to formthe drug/resin complex is a well known technique as shown in U.S. Pat.Nos. 2,990,332 and 4,221,778. In general the drug is mixed with anaqueous suspension of the resin, and the complex is then washed anddried. Adsorption of drug onto the resin may be detected by measuring achange in the pH of the reaction medium, or by measuring a change inconcentration of sodium or drug. The drug/resin complex formed can becollected and washed with ethanol and/or water to insure removal of anyunbound drug. The complexes are usually air-dried in trays at room orelevated temperature. The drug/resin complex has a ratio ofphenylephrine to resin of about 0.25:1 to about 0.65:1, preferably about0.30:1 to about 0.55:1, preferably about 0.35:1 to about 0.45:1.

“Enteric” shall mean being able to be dissolved at a pH of greater thanabout 5.0 or greater than about 5.5 or greater than about 6.0 or thatwhich is found in the intestine.

By “extended release,” it is meant that, after administration, an activeingredient is released from the dosage form in a substantiallycontinuous, regulated manner, and the time for complete release, i.e.,depletion, of the active ingredient from the dosage form is longer thanthat associated with an immediate release dosage form of the same. Typesof extended release include controlled, sustained, prolonged,zero-order, first-order, pulsatile, and the like.

As used herein, “immediate release” means that the dissolutioncharacteristics of at least one active ingredient meet USPspecifications for immediate release tablets containing that activeingredient. An active ingredient having an immediate release propertymay be dissolved in the gastrointestinal contents, with no intention ofdelaying or prolonging the dissolution of the active ingredient.

“Liquid dosage forms” may nonexclusively include suspensions or elixirs,wherein one or more of the active ingredients is dissolved, partiallydissolved or in an undissolved or suspended state.

As used herein, “modified release” shall apply to the altered release ordissolution of an active ingredient in a dissolution medium, such asgastrointestinal fluids. Types of modified release include: 1) extendedrelease; or 2) delayed release. In general, modified release dosageforms are formulated to make the active ingredient(s) available over anextended period of time after ingestion, which thereby allows for areduction in dosing frequency compared to the dosing of the same activeingredient(s) in a conventional dosage form. Modified release dosageforms also permit the use of active ingredient combinations wherein theduration of one active ingredient may differ from the duration ofanother active ingredient.

As used herein, “pharmacodynamics” or “PD” is the study of therelationship between drug concentration at the site of action and theresulting effect.

As used herein, “pharmacokinetics” or “PK” is the study of the timecourse of drug absorption, distribution, metabolism and excretion.

As used herein, the term “phenylephrine” means benzynemethanol,3-hydroxy-α-[(methylamino)methyl], and includes, but is not limited topharmaceutically acceptable salts, esters, isomers or derivativesthereof.

As used herein, a drug “release rate” refers to the quantity of drugreleased from a dosage form per unit time, e.g., milligrams of drugreleased per hour (mg/hr). Drug release rates are calculated under invitro dosage form dissolution testing conditions known in the art. Asused herein, a drug release rate obtained at a specified time “followingadministration” refers to the in vitro drug release rate obtained at thespecified time following commencement of an appropriate dissolutiontest, e.g., those set forth in USP 24 (United States Pharmacopeia 24,United States Pharmacopeia Convention, Inc., Rockville, Md.).

“Semipermeable,” as used herein, shall mean that water can pass through,and other molecules, including salts and the active ingredientsdescribed herein, are allowed to slowly diffuse through such a membranewhen the membrane is in contact with an appropriate dissolution medium,e.g., gastro-intestinal fluids or in-vitro dissolution media.

“Semi-solid dosage forms” shall mean dosage forms which are highlyviscous and share some of the properties of liquids, including but notlimited to (1) having the ability to substantially conform to somethingthat applies pressure to it and causes its shape to deform; and (2)lacking the ability to flow as easily as a liquid. Semi-solid dosageforms also share some of the properties of solids, including but notlimited to having a higher density and a defined shape. Semi-solids maynonexclusively include gels, chewy dosage forms, pectin based chewyforms, confectionery chewy forms, moldable gelatin type of forms.

“Solid dosage forms” shall mean dosage forms which are substantiallysolid at room temperature and have a density of at least about 0.5 g/cc.Solid dosage forms may non exclusively include, agglomerated tablets,capsule-like medicaments, powder or granule filled capsules, powder orgranule filled sachets, compressed tablets, coated tablets, chewabledosage forms, and fast-dissolving dosage forms.

As used herein, “substantially coated” with regard to particles shallmean that less than about 20%, e.g., less than about 15%, or less thanabout 1.0% of the surface area of the particle is exposed, e.g., notcovered, with a desired coating. As used herein, the term “substantiallycovers” or “substantially continuous” when used to describe a coatingmeans that the coating is generally continuous and generally covers theentire surface of the core or underlying layer, so that little to noneof the active ingredient or underlying layer is exposed. The coatingswhich are applied to the particles can be layered wherein each layer isprepared in an aqueous (water based) or organic solvent system and addedin succession until the desired coating level is achieved.

“Therapeutic effect,” as used herein, shall mean any effect or action ofan active ingredient intended to diagnose, treat, cure, mitigate, orprevent disease, or affect the structure or any function of the body.

Specific embodiments of the present invention are illustrated by way ofthe following examples.

This invention is not confined to the specific limitations set forth inthese examples.

EXAMPLES

Phenylephrine extended release particles were developed in order toformulate into liquid and solid dosage forms. The phenylephrine extendedrelease particles can be used to match duration with other actives(particularly pain actives) which may provide a longer duration thanphenylephrine. Such actives include, but are not limited to,acetaminophen, ibuprofen and naproxen and salts and derivatives thereof

Example 1 Preparation of Formulation Containing Coated PhenylephrineExtended Release Particles

A formulation that contains phenylephrine particles coated with apolymer coating was prepared. The formulation, which provides release ofphenylephrine over an extended period of time, has proven to be stableat 25° C./60% RH for 24 months and at 40° C./75% RH for 3 months. Manygranulated formulations of phenylephrine are not stable over time andundergo significant degradation.

A batch of 3.203 kg of coated phenylephrine particles was preparedaccording to the formula in Table 1. The quantitative and batchformulas, respectively, are represented in Table 1.

TABLE 1 Coated Extended Release Phenylephrine Particles¹ Weight/ UnitDose Weight % Weight/ Component (mg) (w/w) Batch (kg) Phenylephrine HClUSP 20.00 5.30 0.1699 Pregelatinized Modified Starch NF 91.22 24.170.7739 Ethyl Acrylate and Methyl 134.66 35.68² 1.1427 MethacrylateCopolymer Dispersion (Eudragit ® NE 30D) NF Ethylcellulose (Ethocel ®Standard 45.33 12.01 0.3846 Premium 10) NF Acetyltributyl Citrate NF9.06 2.40 0.0769 Magnesium Stearate NF 9.06 2.40 0.0769 EthylcelluloseAqueous Dispersion 66.27 17.56² 0.5625 (Aquacoat ECD ®)³ NF ColloidalSilicon Dioxide NF 1.77 0.47 0.0150 Purified Water⁴ USP — — — Acetone⁴NF — — — Isopropyl Alcohol⁴ NF — — — TOTAL 100.00 3.203  ¹A unit dose ofthe particles containing 20 mg phenylephrine HCl is approximately 377.4mg. Actual weight is dependent on the assayed amount of phenylephrineHCl in the particles. ²Solids weight. ³Contains ethylcellulose, cetylalcohol and sodium lauryl sulfate. ⁴Purified water, acetone andisopropyl alcohol are removed during processing.

Layering of Particles:

1. Purified water USP was added to a suitably sized stainless steelcontainer.2. Ethyl acrylate NF and methyl methacrylate copolymer dispersion NF(Eudragit® NE 30D) was added with gentle agitation.3. Phenylephrine HCl USP was added while mixing with agitation andmixed.4. Step 3 mixture was used to coat (layer) pregelatinized modifiedstarch NF.

Drying and Screening:

5. The layered phenylephrine HCl/pregelatinized modified starch fromStep 4 was dried and screened through a #20 screen.Coating of Layered Particles with Ethylcellulose Coating Solution:6. The following were added in the order as they appear to a suitablysized container with gentle agitation: isopropyl alcohol USP, followedby acetone NF, followed by acetyltributyl citrate NF.7. Ethylcellulose NF (Ethocel® Standard Premium 10) was added withagitation and mixed until a clear solution was formed.8. Magnesium stearate was added to the solution with agitation.9. The screened layered phenylephrine/pregelatinized modified starchparticles from Step 5 were coated with the solution from Step 8 using asuitable fluid bed coating unit fitted with a Wurster insert.

Curing:

10. The particles from Step 9 were cured in an oven.Coating of Ethocel® Coated Particles with Eudragit® NE30D and AquacoatECD®:11. Eudragit® NE30D was added followed by purified water USP andethylcellulose aqueous dispersion NF (Aquacoat ECD®) to a suitably sizedcontainer and mixed with gentle agitation.12. The Ethocel® coated layered particles from Step 10 were coated withthe coating solution using a suitable fluid bed coating unit fitted witha Wurster insert.13. The coated particles from Step 12 were mixed with colloidal silicondioxide NF.

Curing:

14. The particles from Step 13 were cured in an oven.

Dissolution Analysis

The coated phenylephrine particles from Step 14 were analyzed fordissolution from 0 to 14 hours using the apparatus described in UnitedStates Pharmacopeia <General Chapter <711>Dissolution>, Apparatus II,rotating paddles, utilizing UV detection at 274 nm. The dissolutionmedia was 750 mL of 0.1N HCl for the first hour and then was 1000 mL ofa 0.05 M sodium phosphate buffer, pH 6.8, for the second to thefourteenth hour. The temperature was 37° C. and the rotation speed was50 rpm. The dissolution showed that the percent of phenylephrinereleased versus a standard prepared at 100% of the amount ofphenylephrine in the formulation was less than or equal to 50% in 1hour, greater than or equal to 30% in 3 hours and greater than or equalto 50% in 8 hours. The method employed is below and the results areshown in Table 2 below.

Dissolution Method USP Apparatus (2 Paddles, 50 Rpm)

1. Verify that the dissolution media temperature has reached the targetvalue (37° C.).2. Weigh out samples equivalent to 45 mg of phenylephrine HCl. Addsamples (onto the surface of the medium solution) to each vesselcontaining 750 mL of 0.1N hydrochloric acid and start the dissolutiontest with the paddle speed at 50 rpm. After 1 hour of operation in 0.1Nhydrochloric acid, complete the 1 hour time point measurement. Proceedimmediately to the buffer stage by adding 250 mL of 0.20 M tribasicsodium phosphate. The pH of the buffer medium is 6.8±0.05.3. Measure the UV absorbance of phenylephrine HCl released in the mediumby using a LEAP fiber optic system with in line probes for UVmeasurement at 274 nm.4. The amount of phenylephrine HCl dissolved can be determined using theUV absorbance of the sample solution under test in comparison with thatof a standard solution at the wavelength of 274 nm. The amount ofphenylephrine HCl dissolved can also be determined using the assaymethod below.

TABLE 2 Time (hours) % Dissolution 1 10%-30% 2 30%-50% 3 50%-70% 460%-80% 6 75%-95% 8  85%-100% 10  90%-100% 12  90%-100% 14  90%-100%

Assay Method Sample Preparation

1. Accurately weigh approximately 1600 mg of phenylephrine HCl particlesand transfer into a 200-mL volumetric flask. (It is recommended to add 1mL of 1% acetic acid/water solution to wet the particles to avoid theformation of solid clumps).2. Add 70 mL of 1% acetic acid/acetonitrile solution; shake the flask ona platform shaker at low speed for 1 hour. Note: swirl the flaskperiodically to remove the particles collected above the solvent level.3. Add about 50 mL of 1% acetic acid/water solution to the flask andcontinuously shake the flask at low speed for 1 hour.4. Dilute to volume with 1% acetic acid/water solution and mix well.5. Filter an aliquot using a 0.45 μm Millipore Millex PVDF filter.Discard the first 1-2 mL of filtrate before collection the filtrate forthe further dilution.6. Pipet 6 mL of the filtrate into a 50-mL volumetric flask, dilute tovolume with 1% acetic acid/water and mix well.

Analysis of Phenylephrine

Inject standards (0.05 mg/mL of phenylephrine HCl in 1% aceticacid/water) and samples onto a suitable HPLC system under conditionssimilar to those suggested below. Parameters may be modified to optimizechromatography. Determine the assay of phenylephrine HCl using the peakareas of the sample solutions under test in comparison with the peakareas of the standard solution.

HPLC Chromatographic Conditions Column Phenomenex Luna SCX, 100 mmlength × 4.6 mm ID, 5 μm particle size, 100 Angstrom pore size MobilePhase 25 mM Sodium Acetate Trihydrate Buffer (pH 4.6):Acetonitrile(65:35, v/v) Mobile Phase Program Isocratic Detector UV, 214 nm FlowRate 2.0 mL/min Injection Volume 100 μL Column Temperature AmbientSuggested Run Time 7 minutes Approx. Retention PHE 5 min Time

Degradation Products Method Sample Preparation

2. Accurately weigh approximately 1600 mg of phenylephrine HCl particlesand transfer into a 200-mL volumetric flask. (It is recommended to add 1mL of 1% Acetic Acid/water Solution to wet the particles to avoid theformation of solid clumps).2. Add 70 mL of 1% acetic acid/acetonitrile solution; shake the flask ona platform shaker at low speed for 1 hour. Note: swirl the flaskperiodically to remove the particles collected above the solvent level.3. Add about 50 mL of 1% acetic acid/water solution to the flask andcontinuously shake the flask at low speed for 1 hour.4. Dilute to volume with 1% acetic acid/water solution and mix well.5. Filter an aliquot using a 0.45 μm Millipore Millex PVDF filter.Discard the first 1-2 mL of filtrate before collection the filtrate forthe further dilution.6. Pipet 6 mL of the filtrate into a 50-mL volumetric flask, dilute tovolume with 1% acetic acid/water and mix well.

Analysis of Phenylephrine

Inject standards (0.00025 mg/mL of phenylephrine HCl in 1% aceticacid/water) and samples onto a suitable HPLC system under conditionssimilar to those suggested below. Parameters may be modified to optimizechromatography Determine the amount of the degradation products ofphenylephrine HCl using the peak areas of the sample solutions undertest in comparison with the peak areas of the standard solution.

HPLC Chromatographic Conditions Column Supelco Ascentis RP-Amide, 250 mmlength × 4.6 mm ID, 5 μm particle size, 100 Angstrom pore size MobilePhase A: [100 mM Ammonium Formate Buffer pH 2.9:Acetonitrile (99:1)] B:[100 mM Ammonium Formate Buffer pH 2.9:Acetonitrile (50:50)] LinearGradient Program Time A (% B Flow (minutes) Volume) (% Volume) MobilePhase 1.0 0 100 0 Program 1.0 10 100 0 1.0 13 91 9 1.0 21 45 55 1.0 3825 75 1.0 43 0 100 1.0 44 100 0 1.0 50 100 0 Detector UV, 270 nmInjection Volume 100 μL Column Ambient Temperature Suggested Run 50minutes Time Approx. Retention 4,6-ISOQUIN 5.4 min Time 4,8-ISOQUIN 6.7min PHE-ONE 9.4 min 3HOBA 25.7 min 

Example 2 Preparation of Coated Phenylephrine Resinate Extended ReleaseParticles

Particles that contain phenylephrine and a cationic exchange resin wereprepared and further coated with a semipermeable membrane. The ratio ofthe amounts of the coating ingredients, which can be varied to someextent, can be, e.g., cellulose acetate:hydroxypropylcellulose 2:1, 3:1,4:1 or 5:1. The coating level, which can be varied to some extent, canbe, e.g., 50%, 45%, 40%, 35%, 30%, 25% or 20% by weight of the coatedparticle. Most of the particles in the starting cation exchange resinhad particle sizes between about 74 μm and about 177 μm (microns).

The phenylephrine resinate particles, which provide release ofphenylephrine over an extended period of time, have proven to be stableat 25° C./60% RH for 24 months and at 40° C./75% RH for 3 months. Manygranulated formulations of phenylephrine are not stable over time andundergo significant degradation.

A batch of 3.846 kg of coated phenylephrine resinate particles wasprepared according to the formula in Table 3. The quantitative formulaand batch formula are represented in Table 3 and Table 4, respectively.

TABLE 3 Coated Phenylephrine Resinate Quantitative Formula Formula A¹Formula B¹ Weight % Component mg/Unit mg/Unit (w/w) Phenylephrine HCLUSP 20.00 15.00 19.50² Sodium Polystyrene Sulfonate 38.32 28.76 45.50USP (most of the particles have a particle size of about 74 μm to about177 μm) Cellulose Acetate NF 22.10 16.59 26.25 Hydroxypropyl CelluloseNF 7.37 5.53 8.75 Acetone NF³ — — — Purified Water USP³ — — — ¹Unitdoses of particles containing 20 mg (A) and 15 mg (B) phenylephrine HClare approximately 84.2 mg and 63.2 mg respectively. Actual weight isdependent on the assayed amount of phenylephrine HCl in the particles.²Quantity represents the free base (1 mg of phenylephrine HCl isequivalent to 0.821 mg of phenylephrine free base). ³Acetone andpurified water are removed during processing.

TABLE 4 Coated Phenylephrine Resinate Batch Formula Component Weight(kg)/Batch Weight % (w/w) Phenylephrine free base¹ 0.750 19.5 SodiumPolystyrene Sulfonate 1.750 45.5 USP (particle size of about 74 μm toabout 177 μm) Cellulose Acetate NF 1.0095 26.25 Hydroxypropyl CelluloseNF 0.3365 8.75 Acetone NF³ — — Purified Water USP³ — — Total 3.846 100.0¹One gram of phenylephrine hydrochloride is equivalent to 0.821 grams ofphenylephrine free base. ²Acetone and purified water are removed duringprocessing.

The coated phenylephrine resinate particles were produced using thefollowing processing steps:

Screening:

1. Sodium polystyrene sulfonate USP having desired particle size waspassed through a 170 mesh screen and the fraction remaining on thescreen was collected.

Washing:

2. Sodium polystyrene sulfonate USP from Step 1 was dispersed inpurified water and mixed.3. While mixing, a portion of the slurry from Step 2 was filtered andwashed with purified water USP. Filtration was continued until most ofthe water was removed.4. The resin was transferred into a container.5. Steps 3 and 4 were repeated until all of the slurry was removed.

Drug Loading:

6. Purified water USP was added into a suitably sized stainless steelcontainer.7. While mixing, phenylephrine HCL was added to the container and mixeduntil dissolved.8. The washed resin from Step 5 was added with continuous mixing andmixed into the slurry.9. While mixing, a portion of the slurry from Step 8 was withdrawn andwashed with purified water USP. Filtration was continued until most ofthe water was removed.10. The washed filtered phenylephrine resinate from Step 9 wastransferred into a container.11. Steps 9 and 10 were repeated until all of the slurry was filtered.

Drying:

12. The phenylephrine resinate was dried.

Preparation of the Coating Solution:

13. Purified water USP and acetone NF were added to an appropriatelysized stainless steel container.14. Hydroxypropylcellulose NF was slowly added to the container andmixed until dissolved. Cellulose acetate NF was slowly added and mixeduntil dissolved.15. Acetone NF was added until the solution was at the desired weight.

Coating:

16. The phenylephrine resinate from Step 12 was coated with coatingsolution from Step 15 in appropriate fluid bed coating equipment fittedwith a Wurster column.17. The coated phenylephrine resinate was discharged into a container.

Drying:

18. The coated phenylephrine resinate was dried.

Screening:

19. The dried coated phenylephrine resinate was screened through a U.S.standard #40 mesh screen and the fraction passing through the screen wascollected.

Dissolution Analysis

The coated phenylephrine resinate particles from Step 19 were analyzedfor dissolution from 0 to 14 hours using the apparatus described inUnited States Pharmacopeia <General Chapter<711>Dissolution>, ApparatusII, rotating paddles, utilizing UV detection at 274 nm. The dissolutionmedia was 750 mL of 0.1N HCl for the first hour and was 1000 mL of a0.05 M sodium phosphate buffer, pH 6.8, the second to the fourteenthhour. The temperature was 37° C. and the rotation speed was 50 rpm. Thedissolution showed that the percent of phenylephrine released versus astandard prepared at 100% of the amount of phenylephrine in theformulation was less than or equal to 50% in 1 hour, greater than orequal to 30% in 3 hours and greater than or equal to 50% in 8 hours. Themethod employed is below and the results are shown in Table 5 below.

Dissolution Method USP Apparatus 2 (Paddles), 50 Rpm

1. Verify that the dissolution media temperature has reached the targetvalue.2. Add sample (onto the surface of the medium solution) to each vesselcontaining 750 mL of 0.1 N hydrochloric acid and start the dissolutiontest with the paddle speed at 50 rpm. After 1 hour of operation in 0.1 Nhydrochloric acid, pull the 1 hour sample, and proceed immediately tothe buffer stage by adding 250 mL of 0.20 M tribasic sodium phosphate.The pH of the media should be 6.8±0.05.3. Pull 10 mL of dissolution sample solutions from each vessel after 1hour, 3 hours, 6 hours (optional), and 8 hours. Filter the samplesolutions through Varian Full Flow Filters (10 μm).4. The amount of phenylephrine dissolved can be determined from UVabsorbance in comparison with that of the standard solution at thewavelength of 274 nm. The amount of phenylephrine dissolved can also bedetermined using the phenylephrine assay method.5. Correct the amount dissolved at 3, 6, and 8 hours by adding theamount pulled at the earlier time points. Use DISSL Program (orequivalent) or manually correct for intermediate sampling.

TABLE 5 Time (hours) % Dissolution 1 20%-40% 2 40%-60% 3 50%-70% 460%-80% 6 75%-95% 8  80%-100% 10  90%-100% 12  90%-100% 14  90%-100%

Example 3 Particle Size Distribution Analysis

Several lots of resin and resin based particles were analyzed forparticle size distribution. The samples included (1) Amberlite™ IRP69resin, commercially available from The DOW Chemical Company, (2)unloaded resin having selected particle sizes (as prepared by Process Aor Process B, respectively), and (3) loaded resinate particles (i.e.,containing phenylephrine). The particle size distribution was analyzedusing approximately 75 grams per sample in an FMC Syntron Sieve analyzer(FMC Technologies, Houston, Tex.), with settings at 90 volts for 11minutes. The sieves were treated with a light dusting of magnesiumstearate to prevent sticking during operation. The results are shown inTables 6 and 7.

Particle size distribution can be analyzed on a smaller scale, using,e.g., an ATM L3P Sonic Sifter (Advantech Manufacturing, New Berlin,Wis.), which operates by using sonic pulses combined with mechanicalagitation, to provide effective separation of particles.

TABLE 6 Particle Size Analysis of Unloaded Resin with “As is” andSelection Process A & B AL AL Lot 1 Lot 2 Lot 3 Lot 4 IRP69 IRP69Process Process Process Process Mesh Size Lot 1¹ Lot 2¹ A² A² B³ B³  80177 μm 0.1% 0.2% 0.1% 0.1% 0.2% 0.0% 100 149 μm 0.2% 0.3% 0.4% 0.4% 2.0%0.2% 120 125 μm 0.8% 0.9% 3.4% 3.4% 19.8% 14.5% 140 105 μm 1.8% 1.7%13.3% 15.1% 35.0% 34.1% 200 74 μm 23.2% 18.2% 80.9% 79.4% 41.7% 50.4%325 44 μm 38.1% 37.4% 1.7% 1.5% 1.3% 0.8% PAN 0 μm 35.8% 41.4% 0.1% 0.0%0.0% 0.0% >149 μm 0.4% 0.5% 0.6% 0.5% 2.2% 0.2% <74 μm 73.9% 78.7% 1.8%1.5% 1.3% 0.8% >44 μm 64.2% 58.6% 99.9% 100.0% 100.0% 100.0% 74-177 μm26.0% 21.1% 98.1% 98.4% 98.6% 99.1% 74-125 μm 24.9% 19.9% 94.2% 94.6%76.8% 84.5% D₁₀ (μm)⁴ 7.7 7.0 76.7 76.8 79.6 78.9 D₅₀ (μm)⁴ 53.4 49.691.1 91.6 108.7 104.1 D₉₀ (μm)⁴ 94.4 91.9 115.5 116.6 139.0 132.4 Mean(μm) 54.8 51.5 94.4 94.6 108.8 105.0 ¹Amberlite ™ IRP69 “As is”commercially available ²Amberlite ™ IRP69 after selecting particle size“Process A” ³Amberlite ™ IRP69 after selecting particle size “Process B”⁴D₁₀, D₅₀ and D₉₀ determined using GRADISTAT, Blott, S. J. and Pye, K.(2001) GRADISTAT: a grain size distribution and statistics package forthe analysis of unconsolidated sediments. Earth Surface Processes andLandforms 26, 1237-1248.

TABLE 7 Particle Size Analysis of Loaded Resin with Selection Process A& B Lot 1 Lot 2 Lot 3 Lot 4.1 Lot 4.2 Lot 4.3 Lot 4.4 Process ProcessProcess Process Process Process Process Mesh Size A¹ A¹ B² B² B² B² B² 80 177 μm 0.2% 0.2% 0.7% 0.1% 0.0% 0.1% 0.1% 100 149 μm 1.1% 1.2% 6.0%1.0% 1.0% 1.1% 1.5% 120 125 μm 7.5% 8.1% 34.4% 33.8% 33.1% 34.9% 36.6%140 105 μm 4.5 32.3% 36.5% 36.7% 38.1% 36.1% 33.2% 200 74 μm 65.8 53.1%22.1% 27.7% 27.2% 26.8% 25.4% 325 44 μm 0.9% 4.2% 0.2% 0.8% 0.6% 1.0%2.6% PAN 0 μm 0.0% 1.0% 0.0% 0.0% 0.0% 0.1% 0.7% >149 μm 1.3% 1.4% 6.7%1.1% 1.0% 1.1% 1.5% <74 μm 0.9% 5.1% 0.2% 0.8% 0.7% 1.1% 3.3% >44 μm100.0% 99.0% 100.0% 100.0% 100.0% 99.9% 99.3% 74-177 μm 98.9% 94.6%99.1% 99.2% 99.3% 98.8% 96.7% 74-125 μm 90.3% 85.3% 58.6% 64.3% 65.3%62.9% 58.6% D₁₀ (μm)³ 77.7 76.4 86.4 83.2 83.5 83.1 81.2 D₅₀ (μm)³ 96.199.5 119.8 116.3 116.2 116.8 117.4 D₉₀ (μm)³ 123.9 124.7 146.5 142.3142.1 142.5 143.1 Mean (μm) 99.8 99.9 120.2 115.3 115.3 115.5 114.7¹Amberlite ™ IRP69 after selecting particle size “Process A”²Amberlite ™ IRP69 after selecting particle size “Process B” ³D₁₀, D₅₀and D₉₀ determined using GRADISTAT, Blott, S. J. and Pye, K. (2001)GRADISTAT: a grain size distribution and statistics package for theanalysis of unconsolidated sediments. Earth Surface Processes andLandforms 26, 1237-1248.

The impact of the drug-resin ratio on the efficiency of drug loading wasobserved. The results are shown in Tables 8 and 9 below.

TABLE 8 Impact of drug-resin ratio on drug loading process forrepresentative drug loading batches Phenylephrine Loading Size MixingDrug-resin free base Efficiency Drug-resin Range Resin Time Ratio (%w/w) (%) Ratio Lot (μm) (kg) (hr) (Slurry) in Resinate of Resinate(Resinate) Lot 4 75-150 10.000 4.5 0.90:1 33.46 67.8% 0.50:1 Process B(Table 6) Lot 3 75-150 8.798 3.0 0.75:1 31.19 73.8% 0.45:1 Process B(Table 6) Lot 4 75-150 10.000 3.0 0.55:1 27.39 83.8% 0.38:1 Process B(Table 6) Lot 4 75-150 10.000 3.0 0.55:1 26.99 82.1% 0.37:1 Process B(Table 6) Lot 4 75-150 10.000 3.0 0.55:1 28.03 86.5% 0.39:1 Process B(Table 6) Lot 4 75-150 9.000 3.0 0.55:1 27.62 84.8% 0.38:1 Process B(Table 6) Lot 4 75-150 9.000 3.0 0.55:1 27.74 85.3% 0.38:1 Process B(Table 6) Larger 212-420  0.500 3.0 0.69:1 30.36 76.7% 0.44:1 particlesize Larger 212-420  4.551 3.0 0.55:1 27.80 85.5% 0.39:1 particle sizeLarger 212-420  4.750 3.0 0.55:1 27.97 86.2% 0.39:1 particle size

TABLE 9 Summary of drug-resin ratio impact on drug loading processPhenylephrine Loading Drug-resin Size Range Mixing Drug-resin free base(%) Efficiency (%) Ratio (μm) Time (hr) Ratio (Slurry)¹ in Resinate ofResinate (Resinate) Comment(s)  75-150 3.0 0.55:1 27.55 84.5% 0.38:1Average of 5 lots 3.0 0.75:1 31.19 73.8% 0.45:1 4.5 0.90:1 33.46 67.8%0.50:1 212-420 3.0 0.55:1 27.89 85.8% 0.39:1 Average of 2 lots 3.00.69:1 30.36 76.7% 0.44:1 ¹Based on phenylephrine HCl in slurry. 2.Based on free base of phenylephrine.

Phenylephrine Assay Method—Measurements for Tables 8 and 9 SamplePreparation

-   1. Accurately weigh suitable amount of coated phenylephrine resinate    sample (containing equivalent of 25 mg of phenylephrine HCl) and    transfer the weighed sample into a 500-mL volumetric flask.-   2. Add 400 mL of diluent (1N HCl); shake the flask on a platform    shaker at low speed for not less than 2 hours.-   3. To ensure that particles do not collect above the solvent level,    periodically rinse particulates into solution with diluent.-   4. Dilute to volume with diluent and mix well.-   5. Filter an aliquot using a 0.45 μm Millipore Millex PVDF syringe    filter, or equivalent. Discard approximately the first 5 mL of    filtrate before collection of the remainder in a HPLC vial for    analysis.

Analysis of Phenylephrine

Inject standards (0.05 mg/mL of phenylephrine HCl in 1 N HCl) andsamples onto a suitable HPLC system under conditions similar to thosesuggested below. Parameters may be modified to optimize chromatography.Analytical results are valid if system suitability specifications aremet.

HPLC Chromatographic Conditions Column Phenomenex Luna SCX, 100 mmlength × 4.6 mm ID, 5 μm particle size, 100 angstrom pore size MobilePhase 25 mM sodium acetate trihydrate buffer (pH 4.6):Acetonitrile(65:35, v/v) Mobile Phase Program Isocratic Detector UV, 214 nm FlowRate 2.0 mL/min Injection Volume 100 μL Column Temperature AmbientSuggested Run Time 7 minutes Approx. Retention PHE 5 min Time

Example 4 Dissolution Analysis of PK Study Material

The coated phenylephrine resinate particles employed in the first PKstudy, the second PK study and the PD study of Example 5 were analyzedfor dissolution from zero to 8 hours using the method described inExample 2. The results are shown in Table 10A below.

TABLE 10A Dissolution Analysis (50 rpm) Coated Phenylephrine ResinateCoated Sample from Phenylephrine PK Study 1 and PK Resinate Study 2 35%Coating Sample from PD Study Level 3:1 Cellulose 40% Coating LevelAcetate NF 3:1 Cellulose Acetate NF Hydroxypropyl Cellulose NFHydroxypropyl Cellulose NF Time (n = 6) (n = 6) point % Released %Released 1 Hour 20-40% 20-40% 3 Hours 50-70% 50-70% 6 Hours 75-95%75-95% 8 Hours  80-100%  80-100%

The coated phenylephrine resinate particles employed in the first PKstudy, the second PK study and the PD study of Example 5 were alsoanalyzed for dissolution from zero to 8 hours using the method describedbelow. The results are shown in Table 10B below.

Dissolution Method USP Apparatus 2 (Paddles), 75 Rpm

1. Verify that the dissolution media temperature has reached the targetvalue.2. Add sample (directly into the medium solution using a suitable tube)to each vessel containing 750 mL of 0.1 N hydrochloric acid and startthe dissolution test with the paddle speed at 75 rpm. After 1 hour ofoperation in 0.1 N hydrochloric acid, pull the 1 hour sample, andproceed immediately to the buffer stage by adding 250 mL of 0.20 Mtribasic sodium phosphate. The pH of the media should be 6.8±0.05.3. Pull 10 mL of dissolution sample solutions from each vessel after 1hour, 3 hours, 6 hours (optional), and 8 hours. Filter the samplesolutions through Varian Full Flow Filters (10 μm).4. Determine the amount of phenylephrine dissolved from UV absorbance incomparison with that of the standard solution at the wavelength of 274nm.

The amount of phenylephrine dissolved can also be determined using thephenylephrine assay method.

5. Correct the amount dissolved at 3, 6, and 8 hours by adding theamount pulled at the earlier time points. Use DISSL Program (orequivalent) or manually correct for intermediate sampling.

TABLE 10B Dissolution Analysis (75 rpm) Coated Phenylephrine ResinateCoated Sample from PK Study 1 Phenylephrine Resinate and PK Study 2Sample from PD Study 35% Coating Level 40% Coating Level 3:1 CelluloseAcetate NF 3:1 Cellulose Acetate NF Hydroxypropyl Cellulose NFHydroxypropyl Cellulose NF Time (n = 6) (n = 6) point % Released %Released 1 Hour 20-40%  20-40%  3 Hours 70-90%  65-85%  6 Hours 80-100%80-100% 8 Hours 90-100% 90-100%

Stability Analysis

The coated phenylephrine resinate particles employed in the first PKstudy and the second PK study of Example 5 were analyzed for stabilityafter storage at 1 month at 25° C. and 60% relative humidity and at 1month at 40° C. and 75% relative humidity. For all samples, the levelsof 3-hydroxybenzaldehyde were less than or equal to 0.5%; the levels ofphenylephrine 4,6 isomer(N-Methyl-4,6-Dihydroxy-1,2,3,4-tetrahydroxyisoquinolone HCL) andphenylephrine 4,8 isomer(N-Methyl-4,8-Dihydroxy-1,2,3,4-tetrahydroxyisoquinolone HCL) were lessthan or equal to 2.0%. The total degradation product quantitated asrelated to phenylephrine was less than or equal to 2.0% at 1 month ineach environment.

Degradation Products Method Sample Preparation for Degradation ProductsMethod

-   -   1. Accurately weigh suitable amount of coated phenylephrine        resinate sample (containing equivalent of 25 mg of phenylephrine        HCl) and transfer the weighed sample into a 500-mL volumetric        flask.    -   2. Add 400 mL of diluent (1N HCl); shake the flask on a platform        shaker at low speed for not less than 2 hours.    -   3. To ensure that particles do not collect above the solvent        level, periodically rinse particulates into solution with        diluent.    -   4. Dilute to volume with diluent and mix well.    -   5. Filter an aliquot using a 0.45 μm Millipore Millex PVDF        syringe filter, or equivalent. Discard approximately the first 5        mL of filtrate before collection of the remainder in a HPLC vial        for analysis.

Analysis of Phenylephrine for Degradation Products Method

Inject standards (0.00025 mg/mL of phenylephrine HCl in 1 N HCl) andsamples onto a suitable HPLC system under conditions similar to thosesuggested below. Parameters may be modified to optimize chromatography.Analytical results are valid if system suitability specifications aremet.

HPLC Chromatographic Conditions Column Supelco Ascentis RP-Amide, 250 mmlength × 4.6 mm ID, 5 μm particle size, 100 Angstrom pore size MobilePhase A: [100 mM Ammonium Formate Buffer pH 2.9:Acetonitrile (99:1)] B:[100 mM Ammonium Formate Buffer pH 2.9:Acetonitrile (50:50)] LinearGradient Program Time A B Flow (minutes) (% Volume) (% Volume) MobilePhase 1.0 0 100 0 Program 1.0 10 100 0 1.0 13 91 9 1.0 21 45 55 1.0 3825 75 1.0 43 0 100 1.0 44 100 0 1.0 50 100 0 Detector UV, 270 nmInjection Volume 100 μL Column Ambient Temperature Suggested Run 50minutes Time Approx. Retention 4,6-ISOQUIN 5.4 min Time 4,8-ISOQUIN 6.7min PHE-ONE 9.4 min 3HOBA 25.7 min 

Example 5 Clinical Studies

Two pharmacokinetic (PK) studies and a pharmacodynamic (PD) study wereconducted.

A. First PK Study

A pilot study was conducted on sixteen subjects to determine thepharmacokinetic profile, bioavailability and metabolism of the coatedextended release phenylephrine particles from Example 1 and the coatedextended release phenylephrine resinate particles from Example 2. Thesubjects were assigned to receive four treatments after an overnightfast. There was a seven day washout between the four periods. In bothcases, coated particles equivalent to a 20 mg phenylephrine HCl dosewere administered in applesauce to healthy subjects. In addition, acombination of the extended release phenylephrine resinate particlesfrom Example 2 and a commercial immediate-release liquid was evaluated.In the combination treatment, coated phenylephrine resinate particlesequal to 15 mg phenylephrine HCl were administered in applesauce, and 10mL of liquid equal to 5 mg phenylephrine HCl was administered by oralsyringe.

The coated extended release phenylephrine particles from Example 1 andthe coated extended release phenylephrine resinate particles fromExample 2 were compared to McNeil-PPC, Inc.'s Non-Drowsy Children'sSudafed PE® Nasal Decongestant liquid (phenylephrine HCl 2.5 mg/5 mL).Table 11 summarizes the treatments in the first PK study.

TABLE 11 Treatment Group Total Dose Over 8 Hours A (test) coated ERphenylephrine resinate particles containing 20 mg phenylephrine B (test)coated ER phenylephrine HCl particles containing 20 mg phenylephrine C(test) coated ER phenylephrine resinate particles containing 15 mgphenylephrine and liquid IR phenylephrine HCl¹ containing 5 mgphenylephrine D (reference) liquid IR phenylephrine HCl containing 10 mgphenylephrine ¹The unit dose of approximately 84.2 mg coated ERphenylephrine resinate particles is equivalent to a 20 mg phenylephrineHCl dose. The unit dose of approximately 63.2 mg coated ER phenylephrineresinate particles is equivalent to a 15 mg phenylephrine HCl dose, andthis latter unit dose was administered with 10 mL phenylephrine liquid2.5 mg/5 mL, for a total of dose equivalent to a 20 mg phenylephrineHCl.

The coated ER phenylephrine resinate particles and the ER phenylephrineHCl particles were administered orally after folding the measured amountinto a 4 oz cup of applesauce just prior to dosing. These single doseswere swallowed without chewing, and followed with 240 mL of water. Thephenylephrine HCl liquid was administered orally using an oral syringe.To standardize the conditions for dosing the reference treatment, thefirst of two oral 10 mg doses of liquid were followed with a 4 oz cup ofapplesauce and 240 mL of water.

Serial blood samples were collected into K3-EDTA tubes at specific timepoints over 8 or 16 hours after dose.

B. Second PK Study

A second pilot study was conducted: (i) to determine if 30 mgphenylephrine can attain similar maximum drug concentrations relative totwo 10 mg doses of immediate-release phenylephrine given 4 hours apart;and (ii) to evaluate the ER PK profile and bioavailability of 20 mgphenylephrine and 1300 mg acetaminophen.

The second pilot study was conducted on twenty subjects to determine thepharmacokinetic profiles, bioavailability and metabolism of (1) acombination of (a) the coated extended release phenylephrine resinateparticles from Example 2 equal to 15 mg phenylephrine HCl, (b) 10 mLphenylephrine liquid equal to 5 mg phenylephrine HCl and (c) 1300 mgextended release acetaminophen; (2) a combination of (a) the coatedextended release phenylephrine resinate particles from Example 2 equalto 22.55 mg phenylephrine HCl and (b) phenylephrine liquid equal to 7.5mg phenylephrine HCl; (3) a combination of (a) phenylephrine liquidequal to 20 mg phenylephrine HCl and (b) 1300 mg extended releaseacetaminophen; and (4) phenylephrine liquid equal to 20 mg phenylephrineHCl. Table 12 summarizes the treatments in the second PK study

TABLE 12 Treatment Group Total Dose Over 8 Hours A (test) coated ERphenylephrine resinate containing 15 mg phenylephrine and liquid IRphenylephrine HCl containing 5 mg phenylephrine and 1300 mg ERacetaminophen² B (test) coated ER phenylephrine resinate containing 22.5mg phenylephrine and liquid IR phenylephrine HCl containing 7.5 mgphenylephrine C (reference) liquid IR phenylephrine HCl containing 20 mgphenylephrine and 1300 mg ER acetaminophen D (reference) liquid IRphenylephrine HCl containing 20 mg phenylephrine ²The extended releaseacetaminophen tablet formulation was the same granulation formulationthat is commercially available in Tylenol ® Arthritis.

Serial blood samples were collected into K3-EDTA tubes at specified timepoints over 12 or 20 hours.

Results

Results for the PK studies appear in FIGS. 1-11 and in Table 13 below.

TABLE 13 Comparison of Mean Parameters for First PK Study A B C D (20 mgPE (20 mg PE (5 IR + 15 mg ER (10 mg IR Q4H × Resinate) HCl) Resinate) 2doses) AUC* 1241.7 1162.6 1237.8 1162.5 (pg-hr/ mL) Cmax 208.4 219.4230.8 458 (pg/mL) Tmax (hr) 2.5 2.8 1.97 Tmax 1 = 0.36 Tmax 2 = 4.54Note: Treatments A, B and C = AUC over 16 hours. Treatment D = AUC over8 hours

-   -   Figures are rounded off

In sum, the results show that:

-   -   The ER-IR blend containing 20 mg phenylephrine had a Cmax that        was 50% of the 10 mg IR dose and an AUCinf that was 15% more        than two 10 mg IR doses (20 mg).    -   The ER-IR blend containing 30 mg phenylephrine had a Cmax that        was 85% of the 10 mg IR dose and an AUCinf that was 61% more        than two 10 mg IR doses (20 mg).    -   The ER-IR Blend containing 20 mg phenylephrine and 1300 mg        acetaminophen had a Cmax that was 80% of the 10 mg phenylephrine        IR dose and an AUCinf that was 22% more than two 10 mg IR doses        (20 mg).

The results demonstrate that the formulation of the present inventionprovides efficacy over an extended period of time.

These results also demonstrate that the formulation of the presentinvention is able to match the duration of extended releaseacetaminophen.

The results also demonstrate that phenylephrine exposure is increasedand phenylephrine PK profile is improved relative to a 10 mg immediaterelease dose of phenylephrine when phenylephrine is combined withacetaminophen. This may be due to competition for gut wall metabolismleading to greater absorption of phenylephrine and no effect onacetaminophen; and extended release formulation providing greaterabsorption of phenylephrine due to avoidance of gut wall metabolism inlower GI tract.

C. Pharmacodynamic Study

A randomized, double-blind, placebo-controlled study was conducted todetermine the efficacy of phenylephrine and phenylephrine-acetaminophenextended release formulations in subjects with congestion and painsymptoms due to upper respiratory tract infections. A 30 mg ER dose, a45 mg ER dose and a 30 mg ER dose co-administered with 1300 mgacetaminophen were assessed and compared to placebo. In each example,the coated ER phenylephrine resinate particles of the invention wereemployed. The 30 mg ER dose, the 45 mg ER dose and the 30 mg ER doseco-administered with 1300 mg acetaminophen each performed well againstplacebo in severity score for (1) stuffy/congested nose; (2) sinuspressure/tenderness; and (3) head congestion from 0 to 12 hours on Day1.

The foregoing examples are not intended to limit the scope of thepresent invention, which may be set out in the claims. In particular,various equivalents and substitutions will be recognized by thoseskilled in the art in view of the foregoing disclosure and these arecontemplated to be within the scope of the invention.

REFERENCES

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1. A method of relieving nasal congestion, comprising administering apharmaceutical formulation; said pharmaceutical formulation comprising adrug-resin complex comprising phenylephrine and a cation polystyrenesulfonate, wherein said cation polystyrene sulfonate comprises particlesizes of about 74 μm an to about 177 μm an prior to being combined withthe phenylephrine.
 2. A method of treating the symptoms of cold,influenza, allergies, or non-allergic rhinitis in a subject in needthereof comprising administering a pharmaceutical formulation; saidpharmaceutical formulation comprising a drug-resin complex comprisingphenylephrine and cation polystyrene sulfonate, wherein said cationpolystyrene sulfonate comprises particle sizes of about 74 μm to about177 μm.
 3. The method of claim 1, wherein the cation is selected fromthe group consisting of sodium, copper, zinc, iron, calcium, strontium,magnesium and lithium.
 4. The method of claim 3, wherein the cation issodium.
 5. The method of claim 4, wherein the drug-resin complex iscoated with a coating.
 6. The method of claim 5, wherein the coatingcomprises a cellulose material.
 7. The method of claim 6, wherein thecellulose material is selected from the group consisting of celluloseacetate and hydroxypropylcellulose.
 8. The method of claim 1, whereinthe pharmaceutical formulation is administered about every 6, 8, 12, 16,20, or 24 hours.
 9. The method of claim 8, wherein the pharmaceuticalformulation is administered about every 12 hours.
 10. The method ofclaim 9, wherein the pharmaceutical formulation is administered aboutevery 8 hours.
 11. A method of maintaining sustained bioavailability ofphenylephrine in a subject, comprising administering a pharmaceuticalformulation comprising a drug-resin complex comprising phenylephrine anda cation polystyrene sulfonate, wherein said cation polystyrenesulfonate comprises particle sizes of about 74 μm to about 177 μm,wherein a concentration of phenylephrine in plasma of the subject is atleast about 20, about 40, about 60, about 80, about 100, about 120,about 140, about 160, about 180, or about 200, pg/mL at about 6, about8, about 12, about 16, about 20, or about 24 hours after ingestion. 12.The method of claim 1, wherein at least about 50% of the particles haveparticle sizes of about 74 μm to about 177 μm.
 13. The method of claim12, wherein at least about 80% of the particles have particle sizes ofabout 74 μm to about 177 μm.
 14. The method of claim 13, wherein atleast about 90% of the particles have particle sizes of about 74 μm toabout 177 μm.
 15. The method of claim 1, wherein less than 15% of theparticles have a particle size less than about 44 μm.